In today’s digital clinical research landscape, the trend is clear: organizations are investing heavily in integrating multiple digital systems—eCRF, ePRO, CTMS, RTSM, and beyond—to streamline workflows and centralize trial data. The assumption? That the more systems you connect, the better your processes will become.
But what if that’s not the case?
At Xolomon, we’re taking a different approach. Instead of building a tangle of integrations between separate platforms, we’ve developed a single, unified system that includes all the essential tools clinical trials need, right out of the box. And the results are changing the game.
The integration illusion
While integration is often marketed as a hallmark of digital maturity, it brings with it a long list of hidden costs and risks:
- Time-consuming implementation involving custom development and vendor coordination
- Data mapping errors and synchronization issues between incompatible systems
- Heavy maintenance loads to keep integrations functional over time
- Security vulnerabilities as data flows through multiple systems and interfaces
For many research teams, what begins as a digital upgrade ends in increased complexity, spiraling costs, and frustrated users.
One platform, all the essentials
Xolomon’s Corporate Plan flips the model. Rather than connecting multiple tools, we provide a centralized eClinical environment where everything is designed to work together natively. Our platform includes:
- eCRF and ePRO design and management tools
- Study and site oversight with built-in CTMS functionalities
- User-friendly dashboards for real-time monitoring
- Built-in compliance with EMA, FDA 21 CFR Part 11, GDPR, and ICH-GCP
- Unlimited users and full support, starting from €200/month per study
The advantage? A seamless experience for both researchers and participants, with fewer technical barriers, reduced implementation timelines, and significantly lower total cost of ownership.
Simplicity that scales
This isn’t just about convenience. Xolomon’s approach directly impacts data quality, study efficiency, and researcher autonomy.
Because all components are integrated from day one, users avoid the friction of jumping between systems. They can set up studies faster, make adjustments in real time, and maintain complete oversight, without needing a team of developers or third-party vendors to “glue” their infrastructure together.
In multicenter trials and international studies, where coordination is critical, this unified environment enables consistent workflows and better collaboration across teams and geographies.
Xolomon: making research accessible
In a time when “more integrations” are often equated with innovation, Xolomon shows that less can be more. Instead of trying to force multiple tools to speak the same language, we built a system where everything already does.
If you’re looking for a smarter, more sustainable way to run your clinical trials without the hidden complexity, Xolomon’s unified platform may be exactly what you need. 📩 Ready to simplify your research? Contact us at info@xolomon.com or visit xolomon.com
